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Pediatric Investigation|September 30, 2024
Neurophenotype and genetic analysis of children with Aicardi-Goutières syndrome in ChinaShen Zhang, Weihua Zhang, Changhong Ding, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 14, 2016
[Clinical effect of atomoxetine hydrochloride in 66 children with narcolepsy]Shen Zhang, Changhong Ding, Husheng Wu, et al.
Genes|May 28, 2022
Novel Loss-of-Function Variants in CHD2 Cause Childhood-Onset Epileptic Encephalopathy in Chinese PatientsXu Wang, Di Cui, Changhong Ding, et al.
Pediatric Neurology|April 10, 2021
Clinical Features and Outcomes of Anti-N-Methyl-d-Aspartate Receptor Encephalitis in Infants and ToddlersChanghong Ren, Weihua Zhang, Xiaotun Ren, et al.
Pediatric Investigation|April 6, 2022
Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow-upWeihua Zhang, Jiuwei Li, Xiuwei Zhuo, et al.
Frontiers in Neurology|September 19, 2022
Oculogyric crisis mimicked epilepsy in a Chinese aromatic L-amino acid decarboxylase-deficiency patient: A case reportHongmei Wang, Jiahong Li, Ji Zhou, et al.
Multiple Sclerosis and Related Disorders|September 12, 2022
Mycophenolate mofetil: An alternative disease-modifying agent for MOG-IgG-associated disorders in childhood: A single-center bidirectional cohort studyJi Zhou, Jiuwei Li, Changhong Ren, et al.
Epilepsia|December 22, 2025
The symmetrical claustrum sign in pediatric febrile infection-related epilepsy syndrome: Diagnostic value and clinical implicationsXiaodi Han, Changhong Ren, Hua Cheng, et al.
Developmental Medicine and Child Neurology|September 15, 2022
Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese childrenJiaping Wang, Fang Fang, Changhong Ding, et al.
Brain & Development|August 27, 2018
A novel DDC gene deletion mutation in two Chinese mainland siblings with aromatic l-amino acid decarboxylase deficiencyLifang Dai, Changhong Ding, Fang Fang
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